FILMARRAY? MENINGITIS/ENCEPHALITIS (ME) PANEL RFIT-ASY-0118

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-02 for FILMARRAY? MENINGITIS/ENCEPHALITIS (ME) PANEL RFIT-ASY-0118 manufactured by Biofire Diagnostics, Llc.

MAUDE Entry Details

Report Number3002773840-2020-00001
MDR Report Key9777456
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-02
Date of Report2020-03-02
Date of Event2020-02-05
Date Mfgr Received2020-02-10
Device Manufacturer Date2019-12-13
Date Added to Maude2020-03-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKRISTEN KANACK
Manufacturer Street515 COLOROW DRIVE
Manufacturer CitySALT LAKE CITY, UT
Manufacturer CountryUS
Manufacturer Phone7366354133
Manufacturer G1BIOFIRE DIAGNOSTICS, LLC
Manufacturer Street515 COLOROW DRIVE
Manufacturer CitySALT LAKE CITY,
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFILMARRAY? MENINGITIS/ENCEPHALITIS (ME) PANEL
Generic NameFILMARRAY? MENINGITIS/ENCEPHALITIS (ME) PANEL
Product CodePLO
Date Received2020-03-02
Model NumberRFIT-ASY-0118
Catalog NumberRFIT-ASY-0118
Lot Number1307219
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOFIRE DIAGNOSTICS, LLC
Manufacturer Address515 COLOROW DRIVE SALT LAKE CITY, UT US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-02

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